galactosamine has been researched along with Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase Deficiency in 4 studies
Timeframe | Studies, this research(%) | All Research% |
---|---|---|
pre-1990 | 4 (100.00) | 18.7374 |
1990's | 0 (0.00) | 18.2507 |
2000's | 0 (0.00) | 29.6817 |
2010's | 0 (0.00) | 24.3611 |
2020's | 0 (0.00) | 2.80 |
Authors | Studies |
---|---|
Elliott, H; Hopwood, JJ | 1 |
Miyawaki, T; Moriya, N; Okuda, N; Taniguchi, N | 1 |
Calatroni, A; Mainardi, E; Moretti, M | 1 |
Calatroni, A; Fossati, G; Sinigaglia, F | 1 |
4 other study(ies) available for galactosamine and Acetyl-CoA:alpha-Glucosaminide N-Acetyltransferase Deficiency
Article | Year |
---|---|
Isolation and characterization of N-acetylglucosamine 6-sulfate from the urine of a patient with Sanfilippo type D syndrome and its occurrence in normal urine.
Topics: Acetylglucosamine; Chromatography; Galactosamine; Glucosamine; Heparitin Sulfate; Humans; Keratan Sulfate; Mucopolysaccharidoses; Mucopolysaccharidosis III; Mucopolysaccharidosis VI | 1983 |
Molecular size difference of urinary heparan sulfates from normal individuals and genetic mucopolysaccharidoses.
Topics: Adolescent; Child; Child, Preschool; Chromatography, Gel; Chromatography, Thin Layer; Electrophoresis, Cellulose Acetate; Galactosamine; Glucosamine; Glycosaminoglycans; Heparitin Sulfate; Humans; Male; Molecular Weight; Mucopolysaccharidoses; Mucopolysaccharidosis I; Mucopolysaccharidosis II; Mucopolysaccharidosis III | 1975 |
[Changes in urinary acid oligosaccharides after transfusion of normal plasma in 2 cases of Sanfilippo's syndrome].
Topics: Blood Transfusion; Child; Galactosamine; Glucosamine; Hexuronic Acids; Humans; Male; Mucopolysaccharidoses; Mucopolysaccharidosis III; Oligosaccharides | 1974 |
[Characteristics of urinary heparan sulfate in 5 cases of Sanfilippo's syndrome].
Topics: Child; Child, Preschool; Female; Galactosamine; Glucosamine; Glycosaminoglycans; Hexuronic Acids; Humans; Male; Mucopolysaccharidoses; Mucopolysaccharidosis III | 1974 |